|Publication number||US7615141 B2|
|Application number||US 10/574,552|
|Publication date||Nov 10, 2009|
|Filing date||Oct 1, 2004|
|Priority date||Oct 3, 2003|
|Also published as||US20070089993, WO2005033798A2, WO2005033798A3|
|Publication number||10574552, 574552, PCT/2004/32638, PCT/US/2004/032638, PCT/US/2004/32638, PCT/US/4/032638, PCT/US/4/32638, PCT/US2004/032638, PCT/US2004/32638, PCT/US2004032638, PCT/US200432638, PCT/US4/032638, PCT/US4/32638, PCT/US4032638, PCT/US432638, US 7615141 B2, US 7615141B2, US-B2-7615141, US7615141 B2, US7615141B2|
|Inventors||Daniel T. Schwartz, John D. Whitaker|
|Original Assignee||University Of Washington|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (6), Referenced by (15), Classifications (23), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application claims the benefit of U.S. Provisional Patent Application No. 60/508,756, filed on Oct. 3, 2003, the disclosure of which is hereby expressly incorporated by reference, and priority from the filing date of which is hereby claimed under 35 U.S.C. § 120.
The invention was made with government support under Grant No. DMII-9978577 awarded by the National Science Foundation. The government has certain rights in the invention.
The present invention relates to electrochemical deposition and, more particularly, to the use of electrochemical deposition for micromanufacturing.
The manufacture of microelectromechanical systems (“MEMS”) is currently impaired not by the microelectronic side of MEMS, but rather by the micromechanical side. Microelectronics is now a mature art—and primarily a two-dimensional one. Micro-mechanics, however, is suffering from a prolonged adolescence, its development having been hindered by the attempts of its parents to make it “wear its sibling's old clothes.” While microelectronic components are substantially two dimensional, it is desired that micromechanical components have significant features in the third dimension. Despite this, the majority of micromechanical devices are produced using the inherently 2D methods of lithography-based microelectronics fabrication. Some of these methods have been tailored to produce structures with significant thickness, for example, LIGA (lithography, electroplating, and molding), and thick UV photolithography for electrodeposition, bulk silicon micromachining, silicon direct bonding, etc., but the drawbacks are still present—namely, the reliance of mask sets and the associated labor when it comes to changing device design (which requires another mask set). Additionally, the three-dimensional complexity attainable with such methods is limited; the number of layers rarely exceeding a few dozen. Finally, these processes must be performed in a cleanroom facility, representing a substantial capital investment for a would-be micromachinist.
We have developed an electrochemical printing system that seeks to remedy the micromachinist's plight. The system is capable of producing two-dimensional multimaterial patterns. In its present form, it is ideally suited for custom bump-plating for high-density interconnect flip chips, as well as printed circuit board metallization and repair. Extending the method to the third dimension requires repeated printing of patterned layers comprised of functional-material along with a sacrificial support material. The ability to print multilayer patterns will have a significant impact on both prototyping and direct custom manufacturing of MEMS devices. A method of using the system for custom three-dimensional packaging is also described.
The MEMS Exchange (www.memsnet.org) cites the two main challenges facing the microelectromechanical systems (“MEMS”) community as—(1) insufficient access to MEMS fabrication facilities; and (2) an entanglement of the MEMS design process with the inherent complexities of current fabrication methodologies. Both of these issues stem from the following fact that conventional mask-based microelectronic fabrication processes are still the predominate means of MEMS prototyping.
These problems lie predominately on the micromechanical side of MEMS. While the mask-based fabrication of essentially two-dimensional microelectronic components is a well-established art, a flexible method for producing the arbitrary 3-D geometries ideal for micromechanical components has yet to be found. This sought-after process would ideally be capable of tailoring not only the geometry, but also the material properties in three dimensions, creating parts from so-called functionally graded materials (“FGMs”). The process must also be compatible with existing IC fabrication methods, especially in regard to the required processing temperatures. In lieu of developing such a tool, the MEMS community has thus far made do by adapting existing mask-based microelectronics fabrication techniques to meet some of the above demands. Specifically, significant z-dimensionality has been achieved using mask-based methods by the following strategies—(a) fabricating consecutive layers one on top of the other (e.g., surface silicon micromachining); (b) bonding individual layers after their respective fabrication (e.g., silicon-direct bonding); and (c) producing substantially thick individual layers, either by additive (e.g., LIGA and UV thick-resist lithography) or subtractive (e.g., bulk silicon micromachining) processes.
Tethering the process to lithographic masks, however, limits the number of layers that can feasibly be incorporated in the micromechanical structure, thus constraining design freedom and three-dimensionality. Design iterations are belabored by the need for a new mask or mask set for each alteration, prolonging the design-test phase of a MEMS product's lifecycle. Furthermore, the mask dependency typically requires that fabrication be conducted in a cleanroom facility, which represents a substantial cost to the designer.
Alternatives to mask-based micromachining are currently being developed, most of which are seeking to embody the tenets of “Solid Freeform Fabrication” (“SFF”). SFF has its origins in Rapid Prototyping, which was defined in the Rapid Prototyping Report, October 1992, as:
One of Rapid Prototyping's central goals is to reduce the time it takes to fabricate a testable device, thus expediting product development. Due to the limited materials available for most rapid prototyping processes, these tests are typically limited to form-fit testing. If the above definition is further extended to producing functional devices with the desired geometry AND material properties (the ideal of which are devices made of functionally graded materials), it becomes SFF, (alternatively referred to as “Direct Fabrication” and/or “Rapid Manufacturing”). Whatever the title, such a process applied to MEMS and available at a comparatively modest cost would give a lithography-wearied MEMS designer reason to rejoice.
The basis behind solid freeform fabrication is layered fabrication, building cross-section upon cross-section until the entire device is constructed. SFF is similar in this regard to mask-based microfabrication; however, this is where the similarity ends. SFF builds the layers rapidly, enabling high resolution in the z-direction and flexibility, producing the layers by fully automated computer control. It is therefore much like desktop printing extended to a third dimension.
Among the techniques being employed to direct-manufacture FGM parts is “3D Printing,” which forms each 2D cross-section of the device by selectively applying liquid binder droplets roughly 100 μm in diameter to a layer of powder. The composition can thus be varied by using different binders in much the same fashion as different inks are applied in inkjet printing. The finished parts, however, can be fragile and porous. Additionally, it may be difficult to remove the excess/nonbound powder from the cavities within the part. Alternately, a CO2 laser can be used to selectively sinter the powder at desired locations, as in Selective Layer Sintering. This process suffers from disadvantages similar to those of 3D Printing, however, in that the resulting part is porous. An additional complication, owing to the necessary heating of the powder, is the potential for thermal distortion of the part. Other processes, which do not involve powder layers, deposit individual droplets of build material to build the device. Shape Deposition Manufacturing does this by depositing 1-5 mm diameter drops of molten metal using a process called “microcasting.” Particular relationships must exist between the sacrificial/retained and retained i/retained i+1 materials' melting points and thermal conductivities in order for both (a) high strength bonding (via melt alloying) to occur between retained materials of different composition, and (b) easy removal of the sacrificial material after the build-up phase. A similar process is Ballistic Particle Manufacturing. The drops in this process are issued from a thermal spray nozzle and thus can have smaller diameters (50-100 μm), but must be selected from a more limited range of materials. One of the more promising FGM-SFF techniques is Laser Assisted Net Shaping, where several jets of metal particles are directed at a high-power laser's focal point. The laser heats the metal powders and causes them to melt and stick onto the substrate, with molten pool diameters ranging from ˝ to 5 times the spot size of the laser. Composition gradients are obtained by varying the respective jets' flow rates during the deposition. A disadvantage associated with all processes involving deposition of molten or uncured materials, however, is the build-up of residual thermal stresses, which can cause warping and delamination in the finished product.
Among the techniques employing electrochemical reactions to direct-manufacture parts is the Electrochemical Fabrication process. This process has yet to sever all ties with masks, making it somewhat inflexible; however, its “instant masks” are far more flexible than ordinary lithographic masks. Electrochemical Fabrication applies these compliant masks directly to the anode (counter electrode) that drives the electrodeposition. An assembly line like process moves the substrate (working electrode) underneath a succession of such masks, which are each pressed to the substrate's surface during electroplating, thus depositing a metallic structure true to the pattern of the instant mask. The mask stamp is then lifted and the deposit backfilled with a second material, and planarized before proceeding to the next instant mask. Lastly and most similar to our disclosed invention, is the localized electrodeposition method of Hunter and Madden. This method employs a sharpened electrode, positioned very near the substrate, to drive an electrodeposition reaction in a confined region immediately beneath the electrode's tip. Their demonstrated embodiment relies on diffusion and migration to deliver the depositing species to the reaction zone and moving the tip in three dimensions results in the creation of a three-dimensional line of nickel. The associated patent (U.S. Pat. No. 5,641,391), however, includes an alternative embodiment wherein a nozzle provides forced convection at the reaction zone.
We propose herein a rapid and flexible method for electrochemically producing two-dimensional multimaterial patterns directly from a computer using bitmap graphics files as the exchange medium. The invention controls the size and location of localized electrochemical reaction zones to produce or remove dots of different materials—a plurality of such dots results in a two-dimensional pattern. The method can be extended to produce complex three-dimensional objects by creating multiple two-dimensional patterns on top of one another and optionally selectively dissolving at least one material from the finished “stack” to give a three-dimensionally complex part.
An electrochemical printer head is disclosed for electrolytically depositing material onto or removing material from a conductive substrate. In a preferred embodiment, the printer head includes a plurality of electrodes, each electrode defining an axial channel therethrough. The electrodes are individually addressable, such that each electrode may be individually energized in an electrical circuit between the electrode, electrolyte and conductive substrate. A high electrical resistance system is provided for distributing the electrolyte to the individual electrodes. For example, a cross-talk inhibition layer may be provided upstream of the electrodes and made from a nonconductive material. The cross-talk inhibition layer having one or more narrow apertures therethrough defines a flow path to the electrodes. It is contemplated that alternatively independent flow systems may be provided to each electrode or to subsets of electrodes. A resolution-defining layer is provided below the plurality of electrodes, the resolution-defining layer having a number of relatively small apertures that provide an outflow path for the electrolyte from the electrode channels. The printer head provides a very high deposition rate and can be used to build, or print, three-dimensional structures. Moreover, by varying the electrolyte flow rate(s), applied power, and relative positions, the physical properties of the deposited material may be varied on the fly, producing a functionally-graded material. For example, a portion of the deposited material may be a material that is readily dissolved or etched away, such that the remaining material forms a desired, complex three-dimensional shape.
An electrochemical printer system utilizing the printer head is also disclosed, the system including a source of pressurized electrolyte, an electrical power source, and a mechanism for containing the substrate and electrolyte and for moving the substrate and the printer head relative to each other.
In an embodiment of the invention, the electrodes are relatively massive and formed from a material, such as stainless steel, that is substantially nonreactive and robust in the electrolyte.
A method for producing a functionally-graded material deposit is also disclosed, the method including the steps of providing a conductive substrate in a container containing a liquid electrolyte, providing an electrochemical printer head having a plurality of electrodes with a channel therethrough, the electrochemical printer head having a surface positioned in close proximity to the conductive substrate, wherein the electrochemical printer includes a plurality of flow paths therethrough, at least some of the flow paths including at least one of the electrode channels, providing electrolyte under pressure to the electrochemical printer head such that electrolyte flows through at least some of the plurality of flow paths and is expelled toward the conductive substrate, selectively applying an electric potential between the conductive substrate and at least one of the plurality of electrodes such that a circuit is formed between the electrode, the electrolyte, and the conductive substrate, and varying the flow rate of the electrolyte through the electrochemical printer head and a parameter of the applied electric potential to produce a functionally graded material deposit.
The foregoing aspects and many of the attendant advantages of this invention will become more readily appreciated as the same become better understood by reference to the following detailed description, when taken in conjunction with the accompanying drawings, wherein:
The present invention will now be described with reference to the figures, wherein like numbers indicate like parts.
A single-pixel prototype embodiment of an electrochemical printing system 100 is shown in
A printer head 130 is attached to the lower end of the head adapter 110. The printer head 130 and the head adapter 110 preferably are made from a relatively inert material that will not react with the electrolyte 112. A small aperture 132 extends through the printer head 130 such that the pressurized electrolyte 112 is expelled from the printer head 130, forming a liquid jet. The printer head 130 is disposed in a container 90 partially filled with electrolyte 112. A conductive substrate 92 is located directly below the printer head 130, such that the fluid jet impinges on the substrate 92. In an embodiment of the invention, the head adapter 110 and the printer head 130 are formed from acrylic, and the small aperture 132 has an exit diameter of around 150 microns. The aperture 132 is widened at the top by drilling partly through the layer to reduce the electrical resistance through the aperture 132.
A current or voltage is applied across the counter electrode 112 and the conductive substrate 92, as indicated schematically by the battery symbol 94. It will now be appreciated by persons of skill in the art of electroplating that an electrical circuit is formed between the counter electrode 120 through the electrolyte 112 (and, in particular, through the jet of electrolyte expelled from the aperture 132) and through the conductive substrate 92. By a well-known electrolytic deposition process, with the appropriate selection of electrolyte 112 and current/voltage levels, a desired deposition of material 96 onto the conductive substrate 92 is achieved. As discussed in more detail below, a mechanism (not shown in
It will be appreciated that the deposition of material at any given time occurs primarily at a very small location directly below the printer head aperture 132, which small spot will sometimes be referred to herein as a pixel. By selectively moving the printer head 130 and/or the conductive substrate 92, the pixel location may be moved to achieve a desired shape in a manner analogous to conventional ink jet printers. Moreover, by making multiple passes over the same location, layers of material may be built up to achieve a complex three-dimensional shape. It has been found through the present invention that the material deposition rate achievable using a small jet (micro jet) of electrolyte at the point of deposition can be surprisingly rapid. Extraordinary build rates greater than 20 microns/second have been achieved, which build rates are ten times faster than some of the best mask-based systems. The extraordinary build rates are achieved by controllably varying the electroplating parameters, such as the electrolyte jet speed, applied voltage/current, printer head speed, and gap between the printer head and the substrate (or deposition material).
Moreover, the material properties of the deposition material may be selectively and purposefully varied on the fly. For example, in an iron-nickel electrolyte (NiFe), by selectively controlling the local electrical current and electrolyte flow rate, the relative iron and nickel composition of the deposition material may be altered on the fly, producing iron-rich depositions in some locations and nickel-rich depositions in other locations. Using known techniques, the iron-rich depositions (sacrificial depositions) may be subsequently preferentially etched away. The iron-rich depositions, therefore, provide mechanical support during the printing process and can then be substantially removed to create complicated three-dimensional shapes.
It will also be appreciated that the present methodology and apparatus (with modifications that will be readily apparent to the person of skill in the art) may be utilized for electrolytic deposition of a very wide range of diverse materials, including, for example, many metals, alloys, semiconductors, ceramics, conducting polymers (such as polyaniline and polypyrrole), and proteins. Electrolytically depositable materials are well known in the art and disclosed in the literature and therefore there is no need to list such materials here.
A multi-pixel electrodeposition printer head 230 will now be described with reference to
The flow distribution layer 235 includes a number of through apertures 236 that provides a fluid path wherein the electrolyte enters a plenum 241 defined by the flow plenum layers 240 The flow distribution layer 235 and plenum 241 provide a generally uniform pressure in the electrolyte prior to encountering the plurality of electrodes 220. The cross-talk inhibition layer 245 is an electrically insulating layer having relatively small diameter apertures 246 therethrough. It will be appreciated by the artisan that the cross-talk inhibition layer 245 greatly increases the electrical resistance between the electrodes 220, thereby reducing the undesirable flow of current between electrodes 220 through the electrolyte, as discussed in more detail below.
The electrodes 220 extend through the epoxy overflow layers 250, the epoxy layers 255, and through apertures 261 in the lead interconnect layer 260. The electrodes are held in place by an epoxy 256 and are electrically connected to individual electrical leads 264 (
The electrolyte enters the plenum 241 in the printer head 230 through the apertures 236 in the flow distribution layer 235 and flows through the apertures 246 in the cross-talk inhibition layer 245, through the channels 222 in the electrodes 220, through the apertures 266 in the flow transition layer 265 and out through the small apertures 271 in the resolution defining layer 270.
In manufacturing this embodiment of the printer head 230, a laser cutting system—for example, the Universal Laser Systems' Model M-25—may be used to precisely cut each layer from the desired materials, although any other suitable fabrication method may be utilized, as is well known in the art. The layers are then bonded together with a pressure-applied bonding layer that may be first precisely laser cut to the desired shape. A plan view of each of the layers, including suitable bonding layers, is shown in
The lead interconnect layer 260 is shown in
The flow transition layer 265 and resolution defining layer 270 are shown in
It will be readily appreciated that an electrochemical printer head may be made with fewer and/or additional layers without departing from the present invention. For example, it has been found beneficial to include a filter layer upstream of the flow distribution layer 235 to inhibit the introduction of particulates and preclude or limit clogging in the printer head 230. Similarly, it will be appreciated by the artisan that rather than utilizing a plenum to provide electrolyte to all of the electrodes, separate electrolyte feeds —for example, using multiple syringe pumps—may be provided to each electrode or to separate groups of electrodes. This would have several advantages, including permitting the use of different electrolytes, further enhancing the flexibility of the system, eliminating cross-talk between the electrodes, and eliminating the need for a plenum and flow distribution layer.
In a preferred embodiment, the printer head 230 is assembled as follows, referring now also to
The epoxy layers 255 are then affixed to either side of the lead interconnect layer 260 using the third bonding layers 253, which are precisely cut from double-backed adhesive polyethylene terephthalate film. Assembly is simplified using 1/16″ stainless steel alignment pins 275.
In a novel aspect of the embodiment disclosed in
In the current version of the printer head 230, the flow distribution layer 235, plenum layer 240, cross-talk inhibition layer 245, epoxy overflow layer 250, epoxy layer 255, and flow transition layer 265 were cut from ⅛ inch thick acrylic sheet with polyimide backing. The resolution-defining layer 270 is cut from a 1-mil thick Mylar® sheet. The apertures 236 in the flow distribution layer 235 and the apertures 266 in the flow transition layer 265 are approximately 0.254 inch in diameter, whereas the apertures 271 in the resolution defining layer 270 are significantly smaller—approximately 0.002 inch in diameter. Although precut bonding layers 238, 248, 253, 268 are shown and may be formed, for example, from a pressure-sensitive or touch-sensitive sheet of bonding material, as is known in the art, it will be appreciated that other layered fabrication methods may be used to construct the printer head 230.
To aid the reader, examples of suitable components utilized in the inventors prototype of the present invention are described below. In particular, it will be appreciated that the selected components discussed below are not intended to limit the present invention, but rather were selected in the prototype development of the present embodiment of the invention.
In the currently preferred prototype, the motion control device 280 is a computer-controllable, three-axis mini-mill.
The software is programmed in National Instruments' LabView 6.1 and integrates control of motion, fluid flow, multiplexing, and voltage/current sourcing and measuring. The software incorporates VI's (Virtual Instruments) issued in National Instruments' Flex-Motion, NI-Switch, and NI-DAQ VI libraries.
A Windows 2000® operating system running on an AMD Athlon-based personal computer serves as the primary controller (not shown). Motion control is accomplished with a MAXNC-5 three-axis mini-mill purchased from MAX-NC (Chandler, Ariz.), in conjunction with National Instruments' PCI-7344 motion controller card and UMI-7764 terminal block. The step/direction signals from the controller card are converted to phase-drive signals using three UCN5804B stepper controller ICs, one for each axis, and routed through a 25-pin D-subminiature connector/cable to the MAXNC-5. A Keithley 2400 SourceMeter (not shown) supplies the current/voltage to the electrochemical print head's pixels and measures the voltage/current during pixel activation. The associated signals are passed to and from the controlling PC through National Instruments' PCI-GPIB card. The user has the choice of operating the Keithley as a simple two-wire power supply or as a three-wire potentiostat/galvanostat with a reference electrode. Multiple or individual pixels are addressed through closing specified switches in National Instruments' SCXI-1127 switching module (not shown). The module is housed in National Instruments' SCXI-1000 four-slot chassis and controlled from the PC's PCI bus using National Instruments' PCI-4021 switch controller card. The Keithley is interfaced to the switching module through the high-voltage analog back plane of the SCXI chassis.
Flow control is accomplished with a four-syringe push-pull syringe pump, Model sp260p, purchased from World Precision Instruments. The controlling PC's serial port communicates with the pump using RS-232 commands.
At the core of the system is the electrochemical print head 230, which is secured to the head adapter 210. The head adapter 210 is attached to the z-axis actuator 286 of the mini-mill motion control device 280. The syringe pump 202 forces electrolyte 212 through a ⅛″ inch OD Teflon® tubing 203. The tubing 203 is attached to the head adapter 210 with a flangeless fitting 204. A circuit is formed from the electrode of the print head 230 through the interstitial electrolyte 212 to the conducting substrate 92. The conducting substrate 92 may be formed, for example, as a glass slide sputtered with TiW/Au The functionally graded part (deposition material) 96 is fabricated optionally including co-deposited sacrificial support material. The substrate 92 is secured to an open-top container 90 that serves as a receptacle for excess electrolyte 212.
Referring again to
In the currently preferred mode of operation, the electrolyte 212 is injected under positive pressure from top to bottom, thereby forming a jet generally at the substrate 92. Alternatively, the electrolyte may be sucked from bottom to top with a negative pressure provided by the syringe pump 202. In either case, both the current density and mass transfer are substantially confined to well-defined regions on the underlying substrate 92. Each “pixel” comprises an independently addressable electrode 220 capable of producing a localized electrochemically formed feature on the substrate 92 underlying the aperture 271 in the resolution-defining layer 270. Thus the printer head 230 can produce small “dots” of electrodepositable material (either anodically or cathodically formed) or, alternately, small regions where material has been electrochemically removed.
Two-dimensional patterns are created as shown in the exemplary sequence shown in
The sequence shown in
The electrochemical printing system of the present invention can create two-dimensional patterns from discrete metal dots. The system is thus ideally suited to custom bump plating for flip-chip interconnects. It is also extendible to the metallization and repair of printed circuit boards.
An electrochemical printing system utilizing the printer head 230 has also been used for rapidly characterizing electrolyte baths. In particular, the system allows for creating arrays of dots, each deposited using a different combination of process parameters (in this case, flow and current). Composition mapping with EDX spectroscopy (or the like) is then used to determine the composition of each dot. This is especially useful for specifying composition (and/or other material properties).
As already mentioned, the present invention is suited to producing three-dimensional structures for MEMS. It has the added ability of incorporating nanostructure into an otherwise micro-scale device. Specifically, modulating the electrolyte flow and/or current density during deposition of a single dot can produce lamellae of different compositions. In the case of thin films, nano- and micro-scale lamellae have been shown to impart favorable and tailorable mechanical properties that are significantly different from that of the bulk, producing films that are tough, flexible, and springy. Moreover, the present invention has the ability to print through crystalline insulating phases, like colloidal and block copolymer films, that coat the substrate, thereby providing three-dimensional nanostructure in each build layer.
The system is flexible, producing parts directly from a series of bitmap images, and relatively inexpensive; these features make micromechanical prototyping more accessible and versatile.
A direct extension of the above application is the ability to produce three-dimensionally intertwined interconnects and packaging molds. The interconnects take the form of a retained material (forming the leads) embedded in a sacrificial support material. Retained material is also used to form the boundary of the package, forming the walls of a mold. After removing the support material, a low-viscosity insulating dielectric resin is used to fill around the interconnects and device, up to the walls of the mold. An initially applied vacuum is applied to remove the bulk of the voids, and a high pressure is subsequently applied during cure. Alternately, air could be used as the dielectric, eliminating the resin impregnation step. The resulting packaged device, however, would be more prone to breaking, as well as electrostatic attractions between the interconnects.
As mentioned, counter electrode dissolution plagued earlier trials with thin-film electrodes. It is contemplated that this dissolution can be advantageously exploited to locally enrich the electrolyte with the dissolution product, which would then be deposited at the substrate beneath the pixel. This holds several advantages over the present method. First, it reduces the amount of products from unwanted counter electrode reactions (e.g., proton enrichment through water hydrolysis). Second, it stands to enable a large deposition rate without increasing the conductivity of the bulk electrolyte. While a large concentration of the depositing species is desired for fast plating rates, the concomitant increase in bath conductivity has the adverse effect of reducing the localizing effects of head geometry. By localizing the concentration increase to the fluid between the counter electrode and the reaction zone, the ohmic effects restricting deposition outside of the desired reaction zone will remain, while the increased concentration at the reaction zone will enable fast deposition rates.
Withdrawing the injected electrolyte near the reaction zone has several advantages. First, it reduces the aforementioned pressure drop experienced by the fluid as it passes through the long and narrow head-substrate gap. Second, it reduces the volume holdup within the system and enables electrolyte changes without manually emptying the excess electrolyte from the reservoir. Third, the reduction in volume holdup is accompanied by a reduction in the area of the substrate that is exposed to the electrolyte. Simultaneous injection and withdrawal thus eliminate further the possibility of reactions occurring outside the designated reaction zone.
The present invention can also be used for three-dimensional composition mapping through localized stripping voltammetry. The tool is operated under negative (sucking) flow and an anodic current is passed from one downstream working electrode to the substrate, dissolving the material directly beneath the pixel. The products of the dissolution are sucked up by the negative flow and swept downstream. An additional electrode placed further downstream than the first is then scanned over a potential range as the dissolution-enriched electrolyte passes over its surface. Monitoring the current vs. voltage allows the user to determine which components are present. If this information is already known, the user sets the electrode at a specific voltage and measures the total charge passed as the enriched solution passes by, thus quantifying the amount of that material present in the deposit. Two-dimensional composition maps are obtained by recording the stripping voltammetry signals as a function of x-y position. After one layer is stripped away, the head is lowered and the next layer scanned in the same fashion. Stacking the consecutive two-dimensional composition maps gives composition information in three dimensions.
While the preferred embodiment of the invention has been illustrated and described, it will be appreciated that various changes can be made therein without departing from the spirit and scope of the invention.
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|U.S. Classification||205/133, 205/118, 204/224.00R|
|International Classification||H05K3/24, C25D17/12, H05K3/22, C25D5/02, G03F|
|Cooperative Classification||H05K3/225, C25D17/12, C25D5/02, C25D1/003, C25D5/08, H05K2203/013, H05K3/241, C25D1/00, C25D5/026|
|European Classification||H05K3/24B, C25D5/08, C25D17/12, C25D17/00, C25D5/02, C25D5/02D|
|Feb 9, 2007||AS||Assignment|
Owner name: WASHINGTON, UNIVERSITY OF, WASHINGTON
Free format text: NUNC PRO TUNC ASSIGNMENT;ASSIGNORS:SCHWARTZ, DANIEL T.;WHITAKER, JOHN D.;REEL/FRAME:018877/0539;SIGNING DATES FROM 20041129 TO 20041201
|Aug 12, 2010||AS||Assignment|
Owner name: NATIONAL SCIENCE FOUNDATION, VIRGINIA
Effective date: 20100217
Free format text: CONFIRMATORY LICENSE;ASSIGNOR:UNIVERSITY OF WASHINGTON;REEL/FRAME:024823/0522
|May 10, 2013||FPAY||Fee payment|
Year of fee payment: 4